A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612496



Internal ID21560801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28902874..28902874hg38UCSC Ensembl
chr3:28944365..28944365hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126215
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612496
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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